HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 989577Generated: October 25, 2026
2-(1,3-Dioxan-2-yl)ethyltriphenylphosphonium bromide → HCID 178447863, compound
https://huagongshe.com/reaction/989577
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 2-(1,3-Dioxan-2-yl)ethyltriphenylphosphonium bromide | HCID 2724168 | — |
| Reactant | Potassium tert-butoxide | HCID 23665647 | — |
| Reactant | HCID 178447904 | HCID 178447904 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 178447863 | HCID 178447863 | — |
Reaction Steps
Under nitrogen gas stream, a mixture of 1330 g (2930 mmol) of 2-(1,3-dioxane-2-yl)ethyltriphenylphosphonium bromide with 6.0 l of THF was cooled down to −30° C., and 303 g (2700 mmol) of t-BuOK was added thereto and stirred for 1 hour. To this mixture was added by drops a solution of 500 g (2250 mmol) of 4-(trans-4-propylcyclohexyl)cyclohexanone in 3.0 l of THF while being maintained at a temperature lower than −30° C. After finishing of the adding, the reaction temperature was gradually raised up to room temperature and they were stirred for further 5 hours. The reaction mixture was filtered with Celite, the solvent was distilled off under a reduced pressure, and the residue was subjected to silica gel column chromatography (eluent: mixed solvent of toluene/ethyl acetate=9/1) to obtain 652 g of a crude 2-(2-(4-(trans-4-propylcyclohexyl)cyclohexylidene)-ethyl-1,3-dioxane.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06458433B1 |
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| Source dataset | uspto-grants-2002_10 |
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| ORD ID | ord-c07abed4bfa04c2bb79183851028d825 |
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| Source note | uspto-grants-2002_10 |
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